Chauffert B, Dumas M, Dubuet A, D'Athis P, Olsson N O
Research Group on Digestive Tumors, INSERM U. 252, Dijon, France.
J Pharm Pharmacol. 1988 Feb;40(2):97-100. doi: 10.1111/j.2042-7158.1988.tb05189.x.
Fluorescence microscopy and high pressure liquid chromatography were used to study the decrease of doxorubicin (DXR) concentrations in the liver, spleen, heart, lung, kidney and skeletal muscle of two strains of rats at various times after a single intravenous injection of the drug (8 mg kg-1). DXR was located within the cell nucleus and was mostly undegraded, it persisted, especially in heart, lungs and spleen where it was detectable 10 days after injection. The DXR/DNA ratio, was used as an index of nuclear fixation of the drug. A major difference in the DXR/DNA ratio between the two strains were observed in heart and spleen results; the DXR/DNA ratio was significantly higher in heart and spleen compared with lung, liver and kidney in both strains.
采用荧光显微镜和高压液相色谱法,研究了两株大鼠单次静脉注射阿霉素(DXR,8mg/kg)后不同时间肝脏、脾脏、心脏、肺、肾脏和骨骼肌中阿霉素浓度的降低情况。DXR定位于细胞核内,且大多未降解,其持续存在,尤其是在心脏、肺和脾脏中,注射后10天仍可检测到。DXR/DNA比值用作药物核固定的指标。在心脏和脾脏的结果中观察到两株大鼠之间DXR/DNA比值存在显著差异;两株大鼠心脏和脾脏中的DXR/DNA比值均显著高于肺、肝脏和肾脏。